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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290177Generated: October 28, 2026

Pyridine → HCID 10817049, compound

https://huagongshe.com/reaction/1290177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 10621762HCID 10621762—
SolventDichloromethaneHCID 6344—
ProductHCID 10817049HCID 1081704988.4%

Reaction Steps

To a solution of 3-bromo-8-(2,6-dichloro-3-methylaminobenzyloxy)-2-methylimidazo[1,2-a]-pyridine (68 mg) and pyridine (0.5 ml) in dichloromethane (2 ml) was added 4-nitrophenyl chloroformate (40 mg) at ambient temperature. After stirring for 1 hour, the mixture was partitioned between dichloromethane and water. The aqueous layer was extracted with dichloromethane twice. The organic layers were combined, washed with water twice and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was crystallized from diethyl ether to give 3-bromo-8-[2,6-dichloro-3-[N-methyl-N-(4-nitrophenoxycarbonyl)amino]benzyloxy]-2-methylimidazo[1,2-a]pyridine (84 mg) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750699
Source datasetuspto-grants-1998_05
ORD IDord-104e6b8a61844841b29e1ea736dbc2ed
Source noteuspto-grants-1998_05